Show HN: A local-first genomic analysis toolkit
https://github.com/emrecolako/savior/
I built this over the weekend after downloading my raw file and realising how much clinically significant data was in there that the company never surfaced for me.The tool parses raw genotype files from 23andMe or AncestryDNA and does the following:Cross-references ~1,500 curated, clinically significant SNP variants across 21 categories (cardiovascular, metabolic, autoimmune, pharmacogenomic,...